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• W1920115684 abstract "Acute encephalitis/encephalopathy (AEE) is a devastating cause of severe neurodevelopmental sequelae or death in children. Assessing ongoing brain injury and predicting outcomes using bedside point-of-care testing is expected to be extremely valuable.For this study, three brain injury markers, S-100B, glial fibrillary acidic protein (GFAP), and tau protein, were measured in early cerebrospinal fluid samples of children with AEE. Subjects comprised three groups: Group 1 (non-AEE control, n = 27); Group 2 (AEE with normal resolution or mild sequelae, n = 13); and Group 3 (AEE with severe sequelae or death, i.e. poor outcome, n = 10).All marker levels were significantly higher in Group 3 than in Group 1 or 2. In Group 3, only S-100B was significantly higher in non-survivors than in survivors. For scoring assessment (range: 0-3 points), the predictive accuracies of 3 points for poor outcomes in children with AEE (i.e. Group 2 and 3, n = 23) were 91% (21/23) for S-100B, 74% (17/23) for GFAP, and 78% (18/23) for tau. When the scores were summed up for S-100B, GFAP, and tau (range: 0-9 points), and for S-100B and tau (range: 0-6 points), the patients with poor outcomes were identified more accurately using the respective thresholds of 6 points and 4 points (96% [22/23] and 100% [23/23], respectively).Our findings suggest that combined measurement and scoring assessment of the markers, especially S-100B and tau, show promise as predictors of clinical outcomes in children with AEE." @default.
• W1920115684 created "2016-06-24" @default.
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• W1920115684 date "2013-06-10" @default.
• W1920115684 modified "2023-10-05" @default.
• W1920115684 title "Prognostic value of brain injury biomarkers in acute encephalitis/encephalopathy" @default.
• W1920115684 cites W1483895285 @default.
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• W1920115684 doi "https://doi.org/10.1111/ped.12094" @default.
• W1920115684 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23480596" @default.
• W1920115684 hasPublicationYear "2013" @default.
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